Unexpected formation of a dimeric cation-anionic complex of hypercoordinated tin in the reaction of bis[(2-oxopyrrolidino)methyl]tin dichloride with AgBF4
被引:5
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作者:
Byliken, SY
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机构:Russian Acad Sci, AN Nesmeyanov Organoelement Cpds Inst, Moscow 117813, Russia
Byliken, SY
Pogozhikh, SA
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机构:Russian Acad Sci, AN Nesmeyanov Organoelement Cpds Inst, Moscow 117813, Russia
Pogozhikh, SA
Shipov, AG
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机构:Russian Acad Sci, AN Nesmeyanov Organoelement Cpds Inst, Moscow 117813, Russia
Shipov, AG
Negrebetskii, VV
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机构:Russian Acad Sci, AN Nesmeyanov Organoelement Cpds Inst, Moscow 117813, Russia
Negrebetskii, VV
Ovchinnikov, YE
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机构:Russian Acad Sci, AN Nesmeyanov Organoelement Cpds Inst, Moscow 117813, Russia
Ovchinnikov, YE
Baukov, YI
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机构:Russian Acad Sci, AN Nesmeyanov Organoelement Cpds Inst, Moscow 117813, Russia
Baukov, YI
机构:
[1] Russian Acad Sci, AN Nesmeyanov Organoelement Cpds Inst, Moscow 117813, Russia
hypercoordinated tin compounds;
intramolecular coordination;
X-ray diffraction analysis;
D O I:
10.1007/BF02495498
中图分类号:
O6 [化学];
学科分类号:
0703 ;
摘要:
A new cation-anionic complex of hypercoordinated tin, {[L2Sn(OH)]+BF4-}(2) (L is a bidentate (2-oxopyrrolidino)methyl C,O-chelating ligand), was obtained by the reaction of L2SnCl2 with AgBF4 and structurally characterized by X-ray diffraction analysis. In crystalline form, the BF4- anions are bound to the dications through O-H...F hydrogen bonds (the H-F distance is 1.78 Angstrom). The octahedral coordination of the Sn atoms is strongly distorted because of a weak additional interaction with solvate molecules of dioxane (the Sn-O distance is 3.16 Angstrom).